Ikeda Y
Department of Anatomy, Tokyo Metropolitan Institute for Neuroscience, Japan.
Acta Paediatr Jpn. 1996 Aug;38(4):412-9. doi: 10.1111/j.1442-200x.1996.tb03516.x.
The orphan nuclear receptor steroidogenic factor 1 (SF-1) was isolated as a transcription factor expressed specifically in the mouse primary steroidogenic tissues. SF-1 expression occurs at the earliest stages of adrenal and gonadal development and the expression pattern is sexually dimorphic in gonads during sexual differentiation. The two hormones required for male differentiation, testosterone and Müllerian-inhibiting substance, are regulated by SF-1. Analyses of knockout mice lacking SF-1 by gene targeting disruption demonstrated that the SF-1-disrupted mice lack adrenal glands and gonads, supporting the suggestion that SF-1 is an essential regulator of the endocrine development and differentiation. Additionally, SF-1 is expressed in the pituitary gonadotropes and the ventrolateral hypothalamic nucleus, which are higher levels of the reproductive regulatory axis, of both adults and embryos. These tissues are also affected in SF-1 knockout mice, indicating that SF-1 plays extended roles at all levels of the reproductive axis, by regulating more genes involved in reproductive function and development.
孤儿核受体类固醇生成因子1(SF-1)作为一种在小鼠主要类固醇生成组织中特异性表达的转录因子被分离出来。SF-1的表达出现在肾上腺和性腺发育的最早阶段,并且在性别分化期间性腺中的表达模式具有性别二态性。雄性分化所需的两种激素,睾酮和苗勒管抑制物质,受SF-1调控。通过基因靶向破坏对缺乏SF-1的基因敲除小鼠进行分析表明,SF-1基因敲除小鼠缺乏肾上腺和性腺,这支持了SF-1是内分泌发育和分化的关键调节因子这一观点。此外,SF-1在垂体促性腺细胞和腹外侧下丘脑核中表达,这两者在成年和胚胎的生殖调节轴中处于较高水平。这些组织在SF-1基因敲除小鼠中也受到影响,表明SF-1通过调控更多参与生殖功能和发育的基因,在生殖轴的各个水平发挥广泛作用。